palmidrol has been researched along with iodoresiniferatoxin in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cristino, L; De Petrocellis, L; Di Marzo, V; Korostynski, M; Makuch, W; Malek, N; Petrosino, S; Przewlocka, B; Slezak, M; Starowicz, K; Zychowska, M | 1 |
Finn, DP; Gaspar, JC; Harhen, B; Madasu, MK; McGowan, F; Okine, BN; Prendergast, C; Roche, M | 1 |
2 other study(ies) available for palmidrol and iodoresiniferatoxin
Article | Year |
---|---|
Full inhibition of spinal FAAH leads to TRPV1-mediated analgesic effects in neuropathic rats and possible lipoxygenase-mediated remodeling of anandamide metabolism.
Topics: Amides; Amidohydrolases; Analgesia; Animals; Arachidonate 15-Lipoxygenase; Arachidonic Acids; Benzamides; Calcium Signaling; Carbamates; Diterpenes; Endocannabinoids; Ethanolamines; Flavanones; Glycerides; HEK293 Cells; Humans; Hyperalgesia; Injections, Spinal; Lipoxygenase Inhibitors; Male; Neuralgia; Oleic Acids; Palmitic Acids; Polyunsaturated Alkamides; Posterior Horn Cells; Rats; Rats, Wistar; Sciatic Nerve; Spinal Cord; TRPV Cation Channels | 2013 |
N-palmitoylethanolamide in the anterior cingulate cortex attenuates inflammatory pain behaviour indirectly via a CB1 receptor-mediated mechanism.
Topics: Amides; Animals; Anti-Inflammatory Agents, Non-Steroidal; Cannabinoid Receptor Antagonists; Cohort Studies; Disease Models, Animal; Diterpenes; Ethanolamines; Fixatives; Formaldehyde; Gyrus Cinguli; Locomotion; Male; Microdissection; Microinjections; Pain; Pain Measurement; Palmitic Acids; PPAR gamma; Proto-Oncogene Proteins c-fos; Rats; Rats, Sprague-Dawley; Receptor, Cannabinoid, CB1 | 2016 |